Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 64175 |
| ensemblid | ENSG00000117385.16 |
| hgncid | 19316 |
| symbol | P3H1 |
| name | prolyl 3-hydroxylase 1 |
| refseq_nuc | NM_022356.4 |
| refseq_prot | NP_071751.3 |
| ensembl_nuc | ENST00000296388.10 |
| ensembl_prot | ENSP00000296388.5 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 42746374 |
| end | 42767028 |
| strand | - |
| ver | v1.2 |
| region | chr1:42746374-42767028 |
| region5000 | chr1:42741374-42772028 |
| regionname0 | P3H1_chr1_42746374_42767028 |
| regionname5000 | P3H1_chr1_42741374_42772028 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 736 | 354 | 87 | 52 | 163 | 12 | 38 | 120 | P3H1_chr1_42741374_42772028 | P3H1 | MAVRA others(731): Show |
chr1 | 42741374 | 42772028 |
| a0002 | 0/0 | 736 | 17 | 1 | 4 | 8 | 1 | 3 | 4 | P3H1_chr1_42741374_42772028 | P3H1 | MAVRA others(731): Show |
chr1 | 42741374 | 42772028 |
| a0003 | 0/0 | 736 | 8 | 4 | 2 | 0 | 0 | 2 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | MAVRA others(731): Show |
chr1 | 42741374 | 42772028 |
| a0004 | 0/0 | 736 | 6 | 0 | 0 | 5 | 1 | 0 | 5 | P3H1_chr1_42741374_42772028 | P3H1 | MAVRA others(731): Show |
chr1 | 42741374 | 42772028 |
| a0005 | 0/0 | 736 | 5 | 2 | 3 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | MAVRA others(731): Show |
chr1 | 42741374 | 42772028 |
| a0006 | 0/0 | 736 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | P3H1_chr1_42741374_42772028 | P3H1 | MAVRA others(731): Show |
chr1 | 42741374 | 42772028 |
| a0007 | 0/0 | 736 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | MAVRA others(731): Show |
chr1 | 42741374 | 42772028 |
| a0008 | 0/0 | 736 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | MAVRA others(731): Show |
chr1 | 42741374 | 42772028 |
| a0009 | 0/0 | 736 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | MAVRA others(731): Show |
chr1 | 42741374 | 42772028 |
| a0010 | 0/0 | 736 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | MAVRA others(731): Show |
chr1 | 42741374 | 42772028 |
| a0011 | 0/0 | 736 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | MAVRA others(731): Show |
chr1 | 42741374 | 42772028 |
| a0012 | 0/0 | 736 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | MAVRA others(731): Show |
chr1 | 42741374 | 42772028 |
| a0013 | 0/0 | 736 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | MAVRA others(731): Show |
chr1 | 42741374 | 42772028 |
| a0014 | 0/0 | 736 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | P3H1_chr1_42741374_42772028 | P3H1 | MAVRA others(731): Show |
chr1 | 42741374 | 42772028 |
| a0015 | 0/0 | 736 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | P3H1_chr1_42741374_42772028 | P3H1 | MAVRA others(731): Show |
chr1 | 42741374 | 42772028 |
| a0016 | 0/0 | 736 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | MAVRA others(731): Show |
chr1 | 42741374 | 42772028 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2208 | 329 | 74 | 51 | 154 | 12 | 36 | P3H1_chr1_42741374_42772028 | P3H1 | ATGGC others(2203): Show |
chr1 | 42741374 | 42772028 | ||
| a0001c0007 | 0/0 | 2208 | 5 | 5 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | ATGGC others(2203): Show |
chr1 | 42741374 | 42772028 | ||
| a0001c0008 | 0/0 | 2208 | 4 | 3 | 1 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | ATGGC others(2203): Show |
chr1 | 42741374 | 42772028 | ||
| a0001c0009 | 0/0 | 2208 | 3 | 0 | 0 | 3 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | ATGGC others(2203): Show |
chr1 | 42741374 | 42772028 | ||
| a0001c0010 | 0/0 | 2208 | 3 | 3 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | ATGGC others(2203): Show |
chr1 | 42741374 | 42772028 | ||
| a0001c0011 | 0/0 | 2208 | 3 | 0 | 0 | 3 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | ATGGC others(2203): Show |
chr1 | 42741374 | 42772028 | ||
| a0001c0013 | 0/0 | 2208 | 2 | 0 | 0 | 0 | 0 | 2 | P3H1_chr1_42741374_42772028 | P3H1 | ATGGC others(2203): Show |
chr1 | 42741374 | 42772028 | ||
| a0001c0014 | 0/0 | 2208 | 2 | 0 | 0 | 2 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | ATGGC others(2203): Show |
chr1 | 42741374 | 42772028 | ||
| a0001c0017 | 0/0 | 2208 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | ATGGC others(2203): Show |
chr1 | 42741374 | 42772028 | ||
| a0001c0023 | 0/0 | 2208 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | ATGGC others(2203): Show |
chr1 | 42741374 | 42772028 | ||
| a0001c0027 | 0/0 | 2208 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | ATGGC others(2203): Show |
chr1 | 42741374 | 42772028 | ||
| a0002c0002 | 0/0 | 2208 | 15 | 0 | 4 | 7 | 1 | 3 | P3H1_chr1_42741374_42772028 | P3H1 | ATGGC others(2203): Show |
chr1 | 42741374 | 42772028 | ||
| a0002c0018 | 0/0 | 2208 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | ATGGC others(2203): Show |
chr1 | 42741374 | 42772028 | ||
| a0002c0028 | 0/0 | 2208 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | ATGGC others(2203): Show |
chr1 | 42741374 | 42772028 | ||
| a0003c0003 | 0/0 | 2208 | 8 | 4 | 2 | 0 | 0 | 2 | P3H1_chr1_42741374_42772028 | P3H1 | ATGGC others(2203): Show |
chr1 | 42741374 | 42772028 | ||
| a0004c0004 | 0/0 | 2208 | 6 | 0 | 0 | 5 | 1 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | ATGGC others(2203): Show |
chr1 | 42741374 | 42772028 | ||
| a0005c0005 | 0/0 | 2208 | 5 | 2 | 3 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | ATGGC others(2203): Show |
chr1 | 42741374 | 42772028 | ||
| a0006c0006 | 0/0 | 2208 | 5 | 0 | 0 | 5 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | ATGGC others(2203): Show |
chr1 | 42741374 | 42772028 | ||
| a0007c0012 | 0/0 | 2208 | 2 | 1 | 1 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | ATGGC others(2203): Show |
chr1 | 42741374 | 42772028 | ||
| a0008c0025 | 0/0 | 2208 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | ATGGC others(2203): Show |
chr1 | 42741374 | 42772028 | ||
| a0009c0021 | 0/0 | 2208 | 1 | 0 | 1 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | ATGGC others(2203): Show |
chr1 | 42741374 | 42772028 | ||
| a0010c0019 | 0/0 | 2208 | 1 | 0 | 1 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | ATGGC others(2203): Show |
chr1 | 42741374 | 42772028 | ||
| a0011c0022 | 0/0 | 2208 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | ATGGC others(2203): Show |
chr1 | 42741374 | 42772028 | ||
| a0012c0026 | 0/0 | 2208 | 1 | 0 | 0 | 0 | 0 | 1 | P3H1_chr1_42741374_42772028 | P3H1 | ATGGC others(2203): Show |
chr1 | 42741374 | 42772028 | ||
| a0013c0024 | 0/0 | 2208 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | ATGGC others(2203): Show |
chr1 | 42741374 | 42772028 | ||
| a0014c0016 | 0/0 | 2208 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | ATGGC others(2203): Show |
chr1 | 42741374 | 42772028 | ||
| a0015c0015 | 0/0 | 2208 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | ATGGC others(2203): Show |
chr1 | 42741374 | 42772028 | ||
| a0016c0020 | 0/0 | 2208 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | ATGGC others(2203): Show |
chr1 | 42741374 | 42772028 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2591 | 209 | 38 | 34 | 103 | 9 | 25 | P3H1_chr1_42741374_42772028 | P3H1 | GTAGG others(2586): Show |
chr1 | 42741374 | 42772028 |
| a0001c0001t0002 | 1/1 | 2591 | 116 | 33 | 17 | 50 | 3 | 11 | P3H1_chr1_42741374_42772028 | P3H1 | GTAGG others(2586): Show |
chr1 | 42741374 | 42772028 |
| a0001c0001t0004 | 0/0 | 2591 | 3 | 3 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | GTAGG others(2586): Show |
chr1 | 42741374 | 42772028 |
| a0001c0001t0006 | 0/0 | 2591 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | GTAGG others(2586): Show |
chr1 | 42741374 | 42772028 |
| a0001c0007t0001 | 0/0 | 2591 | 5 | 5 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | GTAGG others(2586): Show |
chr1 | 42741374 | 42772028 |
| a0001c0008t0001 | 0/0 | 2591 | 4 | 3 | 1 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | GTAGG others(2586): Show |
chr1 | 42741374 | 42772028 |
| a0001c0009t0001 | 0/0 | 2591 | 3 | 0 | 0 | 3 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | GTAGG others(2586): Show |
chr1 | 42741374 | 42772028 |
| a0001c0010t0002 | 0/0 | 2591 | 3 | 3 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | GTAGG others(2586): Show |
chr1 | 42741374 | 42772028 |
| a0001c0011t0005 | 0/0 | 2591 | 3 | 0 | 0 | 3 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | TTAGG others(2586): Show |
chr1 | 42741374 | 42772028 |
| a0001c0013t0001 | 0/0 | 2591 | 2 | 0 | 0 | 0 | 0 | 2 | P3H1_chr1_42741374_42772028 | P3H1 | GTAGG others(2586): Show |
chr1 | 42741374 | 42772028 |
| a0001c0014t0002 | 0/0 | 2591 | 2 | 0 | 0 | 2 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | GTAGG others(2586): Show |
chr1 | 42741374 | 42772028 |
| a0001c0017t0001 | 0/0 | 2591 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | GTAGG others(2586): Show |
chr1 | 42741374 | 42772028 |
| a0001c0023t0001 | 0/0 | 2591 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | GTAGG others(2586): Show |
chr1 | 42741374 | 42772028 |
| a0001c0027t0001 | 0/0 | 2591 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | GTAGG others(2586): Show |
chr1 | 42741374 | 42772028 |
| a0002c0002t0001 | 0/0 | 2591 | 15 | 0 | 4 | 7 | 1 | 3 | P3H1_chr1_42741374_42772028 | P3H1 | GTAGG others(2586): Show |
chr1 | 42741374 | 42772028 |
| a0002c0018t0001 | 0/0 | 2591 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | GTAGG others(2586): Show |
chr1 | 42741374 | 42772028 |
| a0002c0028t0001 | 0/0 | 2591 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | GTAGG others(2586): Show |
chr1 | 42741374 | 42772028 |
| a0003c0003t0003 | 0/0 | 2591 | 8 | 4 | 2 | 0 | 0 | 2 | P3H1_chr1_42741374_42772028 | P3H1 | GTAGG others(2586): Show |
chr1 | 42741374 | 42772028 |
| a0004c0004t0002 | 0/0 | 2591 | 6 | 0 | 0 | 5 | 1 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | GTAGG others(2586): Show |
chr1 | 42741374 | 42772028 |
| a0005c0005t0003 | 0/0 | 2591 | 5 | 2 | 3 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | GTAGG others(2586): Show |
chr1 | 42741374 | 42772028 |
| a0006c0006t0001 | 0/0 | 2591 | 5 | 0 | 0 | 5 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | GTAGG others(2586): Show |
chr1 | 42741374 | 42772028 |
| a0007c0012t0001 | 0/0 | 2591 | 2 | 1 | 1 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | GTAGG others(2586): Show |
chr1 | 42741374 | 42772028 |
| a0008c0025t0002 | 0/0 | 2591 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | GTAGG others(2586): Show |
chr1 | 42741374 | 42772028 |
| a0009c0021t0002 | 0/0 | 2591 | 1 | 0 | 1 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | GTAGG others(2586): Show |
chr1 | 42741374 | 42772028 |
| a0010c0019t0001 | 0/0 | 2591 | 1 | 0 | 1 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | GTAGG others(2586): Show |
chr1 | 42741374 | 42772028 |
| a0011c0022t0002 | 0/0 | 2591 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | GTAGG others(2586): Show |
chr1 | 42741374 | 42772028 |
| a0012c0026t0001 | 0/0 | 2591 | 1 | 0 | 0 | 0 | 0 | 1 | P3H1_chr1_42741374_42772028 | P3H1 | GTAGG others(2586): Show |
chr1 | 42741374 | 42772028 |
| a0013c0024t0002 | 0/0 | 2591 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | GTAGG others(2586): Show |
chr1 | 42741374 | 42772028 |
| a0014c0016t0002 | 0/0 | 2591 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | GTAGG others(2586): Show |
chr1 | 42741374 | 42772028 |
| a0015c0015t0002 | 0/0 | 2591 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | GTAGG others(2586): Show |
chr1 | 42741374 | 42772028 |
| a0016c0020t0001 | 0/0 | 2591 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | GTAGG others(2586): Show |
chr1 | 42741374 | 42772028 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 18 | 2 | 2 | 11 | 2 | 1 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0003 | 0/0 | 17 | 5 | 1 | 10 | 0 | 1 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0004 | 0/0 | 16 | 2 | 9 | 0 | 1 | 4 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0005 | 0/0 | 9 | 0 | 2 | 7 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0006 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0009 | 0/0 | 7 | 2 | 3 | 2 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0010 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0011 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0018 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0027 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0001 | 1/0 | 29 | 1 | 4 | 19 | 1 | 3 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0007 | 0/0 | 9 | 0 | 4 | 5 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0008 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0013 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0015 | 0/0 | 4 | 1 | 1 | 0 | 0 | 2 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0023 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0025 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0044 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0049 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0178 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0004g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0001t0006g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0007t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0007t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0007t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0007t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0007t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0008t0001g0045 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0008t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0008t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0009t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0010t0002g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0010t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0011t0005g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0011t0005g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0013t0001g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0014t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0014t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0017t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0023t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0001c0027t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0002c0002t0001g0012 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0002c0002t0001g0016 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0002c0002t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0002c0018t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0002c0028t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0003c0003t0003g0028 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0003c0003t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0003c0003t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0003c0003t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0003c0003t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0003c0003t0003g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0004c0004t0002g0026 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0004c0004t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0004c0004t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0004c0004t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0005c0005t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0005c0005t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0005c0005t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0005c0005t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0005c0005t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0006c0006t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0006c0006t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0007c0012t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0007c0012t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0008c0025t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0009c0021t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0010c0019t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0011c0022t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0012c0026t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0013c0024t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0014c0016t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0015c0015t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| a0016c0020t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0199 | EUR | GBR | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG00280 | hp1 | a0004 | c0004 | t0002 | g0026 | EUR | FIN | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0099 | EUR | FIN | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0198 | EUR | FIN | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | CHS | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | CHS | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG00597 | hp2 | a0008 | c0025 | t0002 | g0183 | EAS | CHS | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | CHS | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG00639 | hp1 | a0007 | c0012 | t0001 | g0157 | AMR | PUR | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0016 | AMR | PUR | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | CHS | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG00738 | hp1 | a0009 | c0021 | t0002 | g0171 | AMR | PUR | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG00738 | hp2 | a0005 | c0005 | t0003 | g0189 | AMR | PUR | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0159 | AMR | PUR | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0012 | AMR | PUR | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0016 | AMR | PUR | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01109 | hp2 | a0010 | c0019 | t0001 | g0075 | AMR | PUR | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01167 | hp2 | a0005 | c0005 | t0003 | g0071 | AMR | PUR | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01169 | hp2 | a0005 | c0005 | t0003 | g0124 | AMR | PUR | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0135 | AMR | PUR | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01243 | hp1 | a0001 | c0008 | t0001 | g0045 | AMR | PUR | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01243 | hp2 | a0003 | c0003 | t0003 | g0028 | AMR | PUR | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | CLM | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0186 | AMR | CLM | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0155 | AMR | CLM | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0137 | EUR | IBS | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0033 | EUR | IBS | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0200 | EUR | IBS | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0213 | AFR | ACB | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0176 | AFR | ACB | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PEL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0184 | AMR | PEL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01981 | hp1 | a0003 | c0003 | t0003 | g0028 | AMR | PEL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0170 | AMR | PEL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02015 | hp2 | a0002 | c0018 | t0001 | g0148 | EAS | KHV | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | KHV | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | KHV | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0194 | AFR | ACB | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0211 | AFR | ACB | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | KHV | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | KHV | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0207 | AFR | ACB | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | CDX | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | CDX | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02257 | hp2 | a0011 | c0022 | t0002 | g0060 | AFR | ACB | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02280 | hp2 | a0001 | c0027 | t0001 | g0179 | AFR | ACB | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | ACB | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | KHV | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0208 | AFR | GWD | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0016 | SAS | PJL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02647 | hp1 | a0005 | c0005 | t0003 | g0139 | AFR | GWD | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0146 | SAS | PJL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0202 | AFR | GWD | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0212 | AFR | GWD | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02809 | hp1 | a0002 | c0028 | t0001 | g0221 | AFR | GWD | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02809 | hp2 | a0001 | c0007 | t0001 | g0204 | AFR | GWD | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | GWD | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0029 | AFR | GWD | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02896 | hp2 | a0003 | c0003 | t0003 | g0216 | AFR | GWD | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02897 | hp1 | a0003 | c0003 | t0003 | g0219 | AFR | GWD | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ESN | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ESN | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | ESN | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02970 | hp1 | a0001 | c0010 | t0002 | g0030 | AFR | ESN | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02970 | hp2 | a0001 | c0008 | t0001 | g0045 | AFR | ESN | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02976 | hp2 | a0001 | c0007 | t0001 | g0203 | AFR | ESN | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03017 | hp1 | a0003 | c0003 | t0003 | g0028 | SAS | PJL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03098 | hp1 | a0003 | c0003 | t0003 | g0217 | AFR | MSL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | MSL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ESN | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03130 | hp2 | a0001 | c0008 | t0001 | g0161 | AFR | ESN | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ESN | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03195 | hp1 | a0001 | c0007 | t0001 | g0196 | AFR | ESN | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0029 | AFR | ESN | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | MSL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03225 | hp1 | a0007 | c0012 | t0001 | g0162 | AFR | MSL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0145 | SAS | PJL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0029 | AFR | MSL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | MSL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | MSL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0185 | AFR | MSL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0151 | SAS | PJL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03516 | hp1 | a0003 | c0003 | t0003 | g0218 | AFR | ESN | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0149 | SAS | PJL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03654 | hp2 | a0001 | c0013 | t0001 | g0041 | SAS | PJL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0012 | SAS | STU | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | STU | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0044 | SAS | PJL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0125 | SAS | PJL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03831 | hp2 | a0012 | c0026 | t0001 | g0141 | SAS | BEB | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0168 | SAS | BEB | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0015 | SAS | STU | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | STU | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | STU | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | STU | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG04228 | hp1 | a0003 | c0003 | t0003 | g0220 | SAS | STU | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG04228 | hp2 | a0001 | c0013 | t0001 | g0041 | SAS | STU | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18522 | hp2 | a0001 | c0010 | t0002 | g0059 | AFR | YRI | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHB | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHB | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | YRI | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | YRI | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18939 | hp1 | a0004 | c0004 | t0002 | g0026 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18939 | hp2 | a0006 | c0006 | t0001 | g0019 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18940 | hp2 | a0014 | c0016 | t0002 | g0052 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18941 | hp1 | a0001 | c0009 | t0001 | g0017 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18941 | hp2 | a0001 | c0011 | t0005 | g0136 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18948 | hp1 | a0001 | c0017 | t0001 | g0101 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18948 | hp2 | a0006 | c0006 | t0001 | g0034 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18953 | hp1 | a0001 | c0011 | t0005 | g0046 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18954 | hp1 | a0001 | c0009 | t0001 | g0017 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18960 | hp1 | a0001 | c0001 | t0006 | g0081 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18963 | hp2 | a0006 | c0006 | t0001 | g0019 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18970 | hp1 | a0001 | c0014 | t0002 | g0215 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18980 | hp2 | a0001 | c0011 | t0005 | g0046 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18985 | hp2 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18993 | hp2 | a0004 | c0004 | t0002 | g0173 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18995 | hp1 | a0015 | c0015 | t0002 | g0051 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19005 | hp2 | a0001 | c0009 | t0001 | g0017 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0181 | AFR | LWK | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | LWK | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | LWK | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19043 | hp2 | a0001 | c0023 | t0001 | g0150 | AFR | LWK | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19054 | hp1 | a0004 | c0004 | t0002 | g0158 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19056 | hp2 | a0004 | c0004 | t0002 | g0188 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19057 | hp2 | a0006 | c0006 | t0001 | g0034 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19058 | hp1 | a0006 | c0006 | t0001 | g0019 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19059 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19091 | hp1 | a0001 | c0014 | t0002 | g0214 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19240 | hp1 | a0001 | c0010 | t0002 | g0030 | AFR | YRI | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | ASW | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ASW | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0042 | EUR | TSI | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0156 | EUR | TSI | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0016 | EUR | TSI | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | GIH | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | GIH | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02486 | hp2 | a0005 | c0005 | t0003 | g0164 | AFR | ACB | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | ACB | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG02559 | hp2 | a0001 | c0007 | t0001 | g0205 | AFR | ACB | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG03471 | hp2 | a0001 | c0008 | t0001 | g0160 | AFR | MSL | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG06807 | hp1 | a0013 | c0024 | t0002 | g0058 | AFR | USA | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | USA | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18955 | hp1 | a0004 | c0004 | t0002 | g0026 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | USA | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA20300 | hp2 | a0001 | c0007 | t0001 | g0209 | AFR | USA | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0195 | AFR | LWK | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| NA21309 | hp2 | a0016 | c0020 | t0001 | g0085 | AFR | LWK | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0178 | REF | REF | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0001 | REF | REF | P3H1_chr1_42741374_42772028 | P3H1 | chr1 | 42741374 | 42772028 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:42746753 | C | T | 1 | a0011 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.2155G>A | p.Glu719Lys | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 15/15 | 2212/2591 | 2155/2211 | 719/736 | chr1 | 42746753 | |||
| chr1:42746756 | G | C | 1 | a0006 | 5 | NA18939.hp2 NA18948.hp2 NA18963.hp2 others(2): Show |
missense_variant | MODERATE | c.2152C>G | p.Pro718Ala | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 15/15 | 2209/2591 | 2152/2211 | 718/736 | chr1 | 42746756 | |||
| chr1:42747295 | G | T | 1 | a0009 | 1 | HG00738.hp1 | missense_variant | MODERATE | c.2032C>A | p.Leu678Met | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 14/15 | 2089/2591 | 2032/2211 | 678/736 | chr1 | 42747295 | |||
| chr1:42747397 | G | T | 1 | a0004 | 6 | HG00280.hp1 NA18939.hp1 NA18955.hp1 others(3): Show |
missense_variant | MODERATE | c.1930C>A | p.Gln644Lys | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 14/15 | 1987/2591 | 1930/2211 | 644/736 | chr1 | 42747397 | |||
| chr1:42750259 | C | T | 1 | a0002 | 17 | HG00642.hp1 HG01074.hp1 HG01106.hp1 others(14): Show |
missense_variant | MODERATE | c.1647G>A | p.Met549Ile | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 11/15 | 1704/2591 | 1647/2211 | 549/736 | chr1 | 42750259 | |||
| chr1:42752314 | T | C | 1 | a0013 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.1529A>G | p.Asn510Ser | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/15 | 1586/2591 | 1529/2211 | 510/736 | chr1 | 42752314 | |||
| chr1:42752326 | G | C | 1 | a0008 | 1 | HG00597.hp2 | missense_variant | MODERATE | c.1517C>G | p.Pro506Arg | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/15 | 1574/2591 | 1517/2211 | 506/736 | chr1 | 42752326 | |||
| chr1:42752339 | C | G | 1 | a0016 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.1504G>C | p.Gly502Arg | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/15 | 1561/2591 | 1504/2211 | 502/736 | chr1 | 42752339 | |||
| chr1:42752366 | C | G | 1 | a0010 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.1477G>C | p.Ala493Pro | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/15 | 1534/2591 | 1477/2211 | 493/736 | chr1 | 42752366 | |||
| chr1:42757788 | G | A | 1 | a0012 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.1075C>T | p.Arg359Cys | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 5/15 | 1132/2591 | 1075/2211 | 359/736 | chr1 | 42757788 | |||
| chr1:42757818 | C | T | 2 | a0003 a0005 |
13 | HG00738.hp2 HG01167.hp2 HG01169.hp2 others(10): Show |
missense_variant | MODERATE | c.1045G>A | p.Gly349Arg | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 5/15 | 1102/2591 | 1045/2211 | 349/736 | chr1 | 42757818 | |||
| chr1:42762330 | G | T | 1 | a0007 | 2 | HG00639.hp1 HG03225.hp1 |
missense_variant | MODERATE | c.611C>A | p.Pro204His | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 2/15 | 668/2591 | 611/2211 | 204/736 | chr1 | 42762330 | |||
| chr1:42766590 | C | G | 1 | a0014 | 1 | NA18940.hp2 | missense_variant | MODERATE | c.382G>C | p.Ala128Pro | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/15 | 439/2591 | 382/2211 | 128/736 | chr1 | 42766590 | |||
| chr1:42766833 | C | A | 1 | a0003 | 8 | HG01243.hp2 HG01981.hp1 HG02896.hp2 others(5): Show |
missense_variant | MODERATE | c.139G>T | p.Ala47Ser | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/15 | 196/2591 | 139/2211 | 47/736 | chr1 | 42766833 | |||
| chr1:42766891 | C | G | 1 | a0015 | 1 | NA18995.hp1 | missense_variant | MODERATE | c.81G>C | p.Glu27Asp | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/15 | 138/2591 | 81/2211 | 27/736 | chr1 | 42766891 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:42746793 | G | A | 1 | a0001c0023 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.2115C>T | p.Leu705Leu | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 15/15 | 2172/2591 | 2115/2211 | 705/736 | chr1 | 42746793 | |||
| chr1:42748226 | G | A | 2 | a0001c0027 a0007c0012 |
3 | HG00639.hp1 HG02280.hp2 HG03225.hp1 |
synonymous_variant | LOW | c.1812C>T | p.Pro604Pro | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 12/15 | 1869/2591 | 1812/2211 | 604/736 | chr1 | 42748226 | |||
| chr1:42750190 | G | A | 1 | a0001c0010 | 3 | HG02970.hp1 NA18522.hp2 NA19240.hp1 |
synonymous_variant | LOW | c.1716C>T | p.Ile572Ile | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 11/15 | 1773/2591 | 1716/2211 | 572/736 | chr1 | 42750190 | |||
| chr1:42750280 | C | T | 1 | a0001c0013 | 2 | HG03654.hp2 HG04228.hp2 |
synonymous_variant | LOW | c.1626G>A | p.Thr542Thr | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 11/15 | 1683/2591 | 1626/2211 | 542/736 | chr1 | 42750280 | |||
| chr1:42752582 | G | A | 1 | a0001c0011 | 3 | NA18941.hp2 NA18953.hp1 NA18980.hp2 |
synonymous_variant | LOW | c.1428C>T | p.Gly476Gly | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 9/15 | 1485/2591 | 1428/2211 | 476/736 | chr1 | 42752582 | |||
| chr1:42754930 | G | A | 2 | a0001c0027 a0007c0012 |
3 | HG00639.hp1 HG02280.hp2 HG03225.hp1 |
synonymous_variant | LOW | c.1284C>T | p.Ile428Ile | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 8/15 | 1341/2591 | 1284/2211 | 428/736 | chr1 | 42754930 | |||
| chr1:42754981 | C | T | 1 | a0001c0008 | 4 | HG01243.hp1 HG02970.hp2 HG03130.hp2 others(1): Show |
synonymous_variant | LOW | c.1233G>A | p.Arg411Arg | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 8/15 | 1290/2591 | 1233/2211 | 411/736 | chr1 | 42754981 | |||
| chr1:42755173 | C | T | 1 | a0002c0018 | 1 | HG02015.hp2 | synonymous_variant | LOW | c.1215G>A | p.Glu405Glu | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 7/15 | 1272/2591 | 1215/2211 | 405/736 | chr1 | 42755173 | |||
| chr1:42757831 | A | G | 1 | a0001c0017 | 1 | NA18948.hp1 | synonymous_variant | LOW | c.1032T>C | p.Tyr344Tyr | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 5/15 | 1089/2591 | 1032/2211 | 344/736 | chr1 | 42757831 | |||
| chr1:42757837 | G | A | 2 | a0001c0027 a0007c0012 |
3 | HG00639.hp1 HG02280.hp2 HG03225.hp1 |
synonymous_variant | LOW | c.1026C>T | p.Ala342Ala | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 5/15 | 1083/2591 | 1026/2211 | 342/736 | chr1 | 42757837 | |||
| chr1:42757885 | G | A | 1 | a0001c0007 | 5 | HG02559.hp2 HG02809.hp2 HG02976.hp2 others(2): Show |
synonymous_variant | LOW | c.978C>T | p.Thr326Thr | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 5/15 | 1035/2591 | 978/2211 | 326/736 | chr1 | 42757885 | |||
| chr1:42766588 | G | C | 1 | a0014c0016 | 1 | NA18940.hp2 | synonymous_variant | LOW | c.384C>G | p.Ala128Ala | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/15 | 441/2591 | 384/2211 | 128/736 | chr1 | 42766588 | |||
| chr1:42766645 | G | A | 1 | a0001c0014 | 2 | NA18970.hp1 NA19091.hp1 |
synonymous_variant | LOW | c.327C>T | p.Phe109Phe | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/15 | 384/2591 | 327/2211 | 109/736 | chr1 | 42766645 | |||
| chr1:42766753 | C | G | 1 | a0001c0009 | 3 | NA18941.hp1 NA18954.hp1 NA19005.hp2 |
synonymous_variant | LOW | c.219G>C | p.Leu73Leu | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/15 | 276/2591 | 219/2211 | 73/736 | chr1 | 42766753 | |||
| chr1:42766939 | T | C | 1 | a0002c0028 | 1 | HG02809.hp1 | synonymous_variant | LOW | c.33A>G | p.Thr11Thr | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/15 | 90/2591 | 33/2211 | 11/736 | chr1 | 42766939 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:42746382 | A | C | 1 | a0001c0001t0006 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*315T>G | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 15/15 | 315 | chr1 | 42746382 | ||||||
| chr1:42746440 | C | T | 17 | a0001c0001t0001 a0001c0001t0006 a0001c0007t0001 others(14): Show |
254 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(251): Show |
3_prime_UTR_variant | MODIFIER | c.*257G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 15/15 | 257 | chr1 | 42746440 | ||||||
| chr1:42746620 | G | A | 2 | a0003c0003t0003 a0005c0005t0003 |
13 | HG00738.hp2 HG01167.hp2 HG01169.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*77C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 15/15 | 77 | chr1 | 42746620 | ||||||
| chr1:42767016 | G | A | 1 | a0001c0001t0004 | 3 | HG02896.hp1 HG03195.hp2 HG03453.hp1 |
5_prime_UTR_variant | MODIFIER | c.-45C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/15 | 45 | chr1 | 42767016 | ||||||
| chr1:42767028 | C | A | 1 | a0001c0011t0005 | 3 | NA18941.hp2 NA18953.hp1 NA18980.hp2 |
5_prime_UTR_variant | MODIFIER | c.-57G>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/15 | 57 | chr1 | 42767028 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:42747009 | G | A | 10 | a0001c0001t0001g0005 a0001c0001t0001g0032 a0001c0001t0001g0039 others(7): Show |
20 | HG01069.hp2 HG01071.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.2056-157C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 14/14 | chr1 | 42747009 | |||||||
| chr1:42747198 | A | T | 34 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(31): Show |
68 | HG00323.hp2 HG00597.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.2055+74T>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 14/14 | chr1 | 42747198 | |||||||
| chr1:42747202 | C | A | 1 | a0001c0001t0001g0035 | 2 | HG01069.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2055+70G>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 14/14 | chr1 | 42747202 | |||||||
| chr1:42747255 | G | A | 14 | a0001c0010t0002g0030 a0001c0010t0002g0059 a0003c0003t0003g0028 others(11): Show |
17 | HG00738.hp2 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.2055+17C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 14/14 | chr1 | 42747255 | |||||||
| chr1:42747259 | G | C | 2 | a0001c0001t0001g0027 a0001c0001t0001g0190 |
4 | HG01167.hp1 HG03471.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.2055+13C>G | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 14/14 | chr1 | 42747259 | |||||||
| chr1:42747432 | A | C | 10 | a0001c0023t0001g0150 a0002c0002t0001g0012 a0002c0002t0001g0016 others(7): Show |
18 | HG00642.hp1 HG01074.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.1915-20T>G | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 13/14 | chr1 | 42747432 | |||||||
| chr1:42747435 | G | C | 2 | a0001c0001t0002g0024 a0001c0001t0002g0182 |
4 | HG00621.hp1 HG00673.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1915-23C>G | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 13/14 | chr1 | 42747435 | |||||||
| chr1:42747614 | C | T | 11 | a0003c0003t0003g0028 a0003c0003t0003g0216 a0003c0003t0003g0217 others(8): Show |
13 | HG00738.hp2 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.1914+109G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 13/14 | chr1 | 42747614 | |||||||
| chr1:42747828 | C | T | 113 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(110): Show |
220 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.1839-30G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 12/14 | chr1 | 42747828 | |||||||
| chr1:42747865 | C | T | 1 | a0001c0001t0001g0109 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1839-67G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 12/14 | chr1 | 42747865 | |||||||
| chr1:42747937 | C | T | 2 | a0001c0001t0001g0103 a0001c0001t0001g0121 |
2 | NA18972.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1839-139G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 12/14 | chr1 | 42747937 | |||||||
| chr1:42747939 | T | C | 160 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
285 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(282): Show |
intron_variant | MODIFIER | c.1839-141A>G | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 12/14 | chr1 | 42747939 | |||||||
| chr1:42748003 | G | A | 1 | a0001c0001t0002g0168 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1838+197C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 12/14 | chr1 | 42748003 | |||||||
| chr1:42748018 | C | T | 8 | a0001c0007t0001g0196 a0001c0007t0001g0203 a0001c0007t0001g0204 others(5): Show |
9 | HG01243.hp1 HG02559.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1838+182G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 12/14 | chr1 | 42748018 | |||||||
| chr1:42748126 | A | G | 34 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(31): Show |
68 | HG00323.hp2 HG00597.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.1838+74T>C | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 12/14 | chr1 | 42748126 | |||||||
| chr1:42748134 | G | T | 8 | a0001c0007t0001g0196 a0001c0007t0001g0203 a0001c0007t0001g0204 others(5): Show |
9 | HG01243.hp1 HG02559.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1838+66C>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 12/14 | chr1 | 42748134 | |||||||
| chr1:42748321 | G | A | 1 | a0001c0001t0002g0193 | 1 | NA18998.hp1 | splice_region_variant&intron_variant | LOW | c.1721-4C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 11/14 | chr1 | 42748321 | |||||||
| chr1:42748418 | C | T | 2 | a0001c0001t0001g0027 a0001c0001t0001g0190 |
4 | HG01167.hp1 HG03471.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1721-101G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 11/14 | chr1 | 42748418 | |||||||
| chr1:42748660 | C | T | 1 | a0001c0001t0002g0181 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1721-343G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 11/14 | chr1 | 42748660 | |||||||
| chr1:42748876 | C | T | 5 | a0001c0001t0002g0013 a0001c0001t0002g0185 a0001c0001t0002g0202 others(2): Show |
9 | HG02145.hp1 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1721-559G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 11/14 | chr1 | 42748876 | |||||||
| chr1:42749012 | C | T | 109 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(106): Show |
215 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.1721-695G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 11/14 | chr1 | 42749012 | |||||||
| chr1:42749145 | C | T | 4 | a0001c0007t0001g0196 a0001c0007t0001g0203 a0001c0007t0001g0205 others(1): Show |
4 | HG02559.hp2 HG02976.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1721-828G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 11/14 | chr1 | 42749145 | |||||||
| chr1:42749151 | G | A | 1 | a0001c0008t0001g0045 | 2 | HG01243.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1721-834C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 11/14 | chr1 | 42749151 | |||||||
| chr1:42749159 | C | T | 3 | a0001c0008t0001g0045 a0001c0008t0001g0160 a0001c0008t0001g0161 |
4 | HG01243.hp1 HG02970.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1721-842G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 11/14 | chr1 | 42749159 | |||||||
| chr1:42749212 | C | T | 1 | a0013c0024t0002g0058 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1721-895G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 11/14 | chr1 | 42749212 | |||||||
| chr1:42749326 | G | A | 1 | a0001c0001t0002g0134 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1720+860C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 11/14 | chr1 | 42749326 | |||||||
| chr1:42749380 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1720+806G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 11/14 | chr1 | 42749380 | |||||||
| chr1:42749381 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1720+805C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 11/14 | chr1 | 42749381 | |||||||
| chr1:42749507 | C | T | 3 | a0001c0027t0001g0179 a0007c0012t0001g0157 a0007c0012t0001g0162 |
3 | HG00639.hp1 HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1720+679G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 11/14 | chr1 | 42749507 | |||||||
| chr1:42749703 | G | A | 1 | a0001c0001t0002g0134 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1720+483C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 11/14 | chr1 | 42749703 | |||||||
| chr1:42749756 | T | TTTG | 4 | a0001c0027t0001g0179 a0007c0012t0001g0157 a0007c0012t0001g0162 others(1): Show |
4 | HG00639.hp1 HG02280.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1720+427_1720+429d others(5): Show |
P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 11/14 | chr1 | 42749756 | |||||||
| chr1:42749756 | TTTG | T | 128 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(125): Show |
238 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.1720+427_1720+429d others(5): Show |
P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 11/14 | chr1 | 42749756 | |||||||
| chr1:42749887 | T | C | 3 | a0001c0027t0001g0179 a0007c0012t0001g0157 a0007c0012t0001g0162 |
3 | HG00639.hp1 HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1720+299A>G | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 11/14 | chr1 | 42749887 | |||||||
| chr1:42749902 | C | T | 1 | a0001c0001t0002g0134 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1720+284G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 11/14 | chr1 | 42749902 | |||||||
| chr1:42749925 | G | A | 3 | a0001c0008t0001g0045 a0001c0008t0001g0160 a0001c0008t0001g0161 |
4 | HG01243.hp1 HG02970.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1720+261C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 11/14 | chr1 | 42749925 | |||||||
| chr1:42749934 | G | T | 1 | a0001c0001t0001g0086 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1720+252C>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 11/14 | chr1 | 42749934 | |||||||
| chr1:42749945 | C | T | 1 | a0007c0012t0001g0162 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1720+241G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 11/14 | chr1 | 42749945 | |||||||
| chr1:42750134 | G | A | 3 | a0001c0027t0001g0179 a0007c0012t0001g0157 a0007c0012t0001g0162 |
3 | HG00639.hp1 HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1720+52C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 11/14 | chr1 | 42750134 | |||||||
| chr1:42750463 | G | A | 1 | a0001c0014t0002g0215 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1570-127C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42750463 | |||||||
| chr1:42750491 | G | A | 2 | a0001c0001t0002g0134 a0001c0027t0001g0179 |
2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1570-155C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42750491 | |||||||
| chr1:42750512 | A | G | 10 | a0001c0023t0001g0150 a0002c0002t0001g0012 a0002c0002t0001g0016 others(7): Show |
18 | HG00642.hp1 HG01074.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.1570-176T>C | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42750512 | |||||||
| chr1:42750520 | C | T | 7 | a0001c0001t0002g0057 a0001c0001t0002g0181 a0001c0001t0002g0211 others(4): Show |
9 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1570-184G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42750520 | |||||||
| chr1:42750522 | C | T | 1 | a0001c0001t0001g0094 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1570-186G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42750522 | |||||||
| chr1:42750539 | A | G | 3 | a0001c0001t0001g0063 a0001c0001t0001g0090 a0001c0001t0001g0091 |
3 | HG03490.hp2 HG03491.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1570-203T>C | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42750539 | |||||||
| chr1:42750556 | CGTCCGGG others(162): Show |
C | 10 | a0003c0003t0003g0028 a0003c0003t0003g0216 a0003c0003t0003g0217 others(7): Show |
12 | HG00738.hp2 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.1570-389_1570-221d others(2): Show |
P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42750556 | |||||||
| chr1:42750621 | C | T | 3 | a0001c0010t0002g0030 a0001c0010t0002g0059 a0013c0024t0002g0058 |
4 | HG02970.hp1 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1570-285G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42750621 | |||||||
| chr1:42750630 | ACCCCGTC others(35): Show |
A | 1 | a0001c0001t0001g0002 | 2 | HG02818.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1570-336_1570-295d others(44): Show |
P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42750630 | |||||||
| chr1:42750634 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1570-298G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42750634 | |||||||
| chr1:42750649 | C | CG | 100 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(97): Show |
178 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.1570-314_1570-313i others(3): Show |
P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42750649 | |||||||
| chr1:42750649 | C | CGG | 14 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0109 others(11): Show |
22 | HG01074.hp1 HG01106.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1570-314_1570-313i others(4): Show |
P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42750649 | |||||||
| chr1:42750650 | C | G | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.1570-314G>C | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42750650 | |||||||
| chr1:42750655 | G | GA | 8 | a0001c0007t0001g0196 a0001c0007t0001g0203 a0001c0007t0001g0204 others(5): Show |
9 | HG01243.hp1 HG02559.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1570-320_1570-319i others(3): Show |
P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42750655 | |||||||
| chr1:42750656 | G | T | 2 | a0001c0001t0001g0004 a0007c0012t0001g0162 |
2 | HG02109.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1570-320C>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42750656 | |||||||
| chr1:42750657 | G | C | 2 | a0001c0001t0001g0002 a0001c0001t0001g0130 |
2 | NA18982.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1570-321C>G | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42750657 | |||||||
| chr1:42750659 | T | G | 164 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
294 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.1570-323A>C | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42750659 | |||||||
| chr1:42750660 | G | C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0094 |
2 | HG00438.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.1570-324C>G | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42750660 | |||||||
| chr1:42750663 | C | T | 4 | a0001c0010t0002g0030 a0001c0010t0002g0059 a0005c0005t0003g0139 others(1): Show |
5 | HG02647.hp1 HG02970.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1570-327G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42750663 | |||||||
| chr1:42750671 | C | A | 5 | a0001c0001t0002g0013 a0001c0001t0002g0185 a0001c0001t0002g0202 others(2): Show |
9 | HG02145.hp1 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1570-335G>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42750671 | |||||||
| chr1:42750677 | G | A | 1 | a0001c0001t0002g0134 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1570-341C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42750677 | |||||||
| chr1:42750712 | C | T | 2 | a0001c0001t0002g0048 a0001c0001t0002g0194 |
3 | HG02055.hp1 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1570-376G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42750712 | |||||||
| chr1:42750713 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1570-377C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42750713 | |||||||
| chr1:42750716 | C | A | 1 | a0001c0013t0001g0041 | 2 | HG03654.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1570-380G>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42750716 | |||||||
| chr1:42750729 | C | T | 1 | a0001c0001t0002g0134 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1570-393G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42750729 | |||||||
| chr1:42750744 | G | A | 2 | a0001c0001t0002g0166 a0001c0001t0002g0202 |
2 | HG02717.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.1570-408C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42750744 | |||||||
| chr1:42750757 | CGCCCCTA others(119): Show |
C | 1 | a0001c0001t0001g0104 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1570-547_1570-422d others(2): Show |
P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42750757 | |||||||
| chr1:42750803 | G | A | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
254 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.1570-467C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42750803 | |||||||
| chr1:42750843 | A | G | 10 | a0003c0003t0003g0028 a0003c0003t0003g0216 a0003c0003t0003g0217 others(7): Show |
12 | HG00738.hp2 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.1570-507T>C | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42750843 | |||||||
| chr1:42750958 | C | A | 1 | a0001c0001t0002g0159 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1570-622G>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42750958 | |||||||
| chr1:42750974 | G | A | 1 | a0001c0001t0001g0102 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1570-638C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42750974 | |||||||
| chr1:42750996 | C | T | 8 | a0001c0001t0002g0057 a0001c0001t0002g0211 a0001c0001t0002g0212 others(5): Show |
9 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1570-660G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42750996 | |||||||
| chr1:42751010 | C | T | 4 | a0003c0003t0003g0028 a0003c0003t0003g0216 a0003c0003t0003g0219 others(1): Show |
6 | HG01243.hp2 HG01981.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1570-674G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42751010 | |||||||
| chr1:42751044 | A | G | 157 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.1570-708T>C | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42751044 | |||||||
| chr1:42751055 | C | T | 2 | a0002c0002t0001g0016 a0002c0002t0001g0186 |
5 | HG00642.hp1 HG01106.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.1570-719G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42751055 | |||||||
| chr1:42751100 | G | A | 2 | a0001c0001t0001g0038 a0001c0001t0001g0072 |
3 | HG02080.hp1 NA18960.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1570-764C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42751100 | |||||||
| chr1:42751102 | C | T | 1 | a0001c0001t0002g0172 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1570-766G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42751102 | |||||||
| chr1:42751108 | C | T | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
255 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.1570-772G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42751108 | |||||||
| chr1:42751126 | A | T | 1 | a0009c0021t0002g0171 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1570-790T>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42751126 | |||||||
| chr1:42751378 | G | A | 2 | a0001c0001t0002g0174 a0001c0001t0002g0176 |
2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1569+896C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42751378 | |||||||
| chr1:42751532 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1569+742G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42751532 | |||||||
| chr1:42751554 | A | G | 1 | a0001c0023t0001g0150 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1569+720T>C | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42751554 | |||||||
| chr1:42751565 | TA | T | 4 | a0001c0007t0001g0204 a0001c0008t0001g0045 a0001c0008t0001g0160 others(1): Show |
5 | HG01243.hp1 HG02809.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1569+708delT | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42751565 | |||||||
| chr1:42751568 | A | AAAAT | 14 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0042 others(11): Show |
32 | HG00140.hp1 HG00140.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.1569+705_1569+706i others(6): Show |
P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42751568 | |||||||
| chr1:42751568 | A | AAAATAAA others(5): Show |
1 | a0001c0001t0001g0138 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1569+705_1569+706i others(14): Show |
P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42751568 | |||||||
| chr1:42751572 | A | T | 115 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(112): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.1569+702T>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42751572 | |||||||
| chr1:42751575 | AT | A | 15 | a0001c0001t0002g0195 a0001c0001t0002g0213 a0001c0007t0001g0196 others(12): Show |
23 | HG00642.hp1 HG01074.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.1569+698delA | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42751575 | |||||||
| chr1:42751576 | T | A | 60 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0008 others(57): Show |
105 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.1569+698A>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42751576 | |||||||
| chr1:42751579 | A | T | 1 | a0001c0023t0001g0150 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1569+695T>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42751579 | |||||||
| chr1:42751580 | T | A | 12 | a0001c0001t0002g0025 a0001c0001t0002g0053 a0001c0001t0002g0168 others(9): Show |
14 | HG00639.hp1 HG01884.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.1569+694A>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42751580 | |||||||
| chr1:42751584 | T | A | 1 | a0001c0001t0002g0054 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1569+690A>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42751584 | |||||||
| chr1:42751584 | T | TA | 9 | a0002c0002t0001g0012 a0002c0002t0001g0016 a0002c0002t0001g0043 others(6): Show |
17 | HG00642.hp1 HG01074.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.1569+689dupT | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42751584 | |||||||
| chr1:42751600 | T | A | 1 | a0001c0001t0001g0191 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1569+674A>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42751600 | |||||||
| chr1:42751623 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1569+651T>C | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42751623 | |||||||
| chr1:42751744 | T | A | 11 | a0001c0001t0001g0006 a0001c0001t0001g0069 a0001c0001t0001g0079 others(8): Show |
22 | HG00408.hp1 HG00423.hp1 HG01952.hp2 others(19): Show |
intron_variant | MODIFIER | c.1569+530A>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42751744 | |||||||
| chr1:42751787 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1569+487C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42751787 | |||||||
| chr1:42751800 | T | C | 2 | a0001c0001t0001g0027 a0001c0001t0001g0190 |
4 | HG01167.hp1 HG03471.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1569+474A>G | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42751800 | |||||||
| chr1:42751853 | A | G | 1 | a0001c0001t0002g0156 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1569+421T>C | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42751853 | |||||||
| chr1:42751874 | C | T | 1 | a0008c0025t0002g0183 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1569+400G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42751874 | |||||||
| chr1:42751958 | A | C | 1 | a0001c0023t0001g0150 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1569+316T>G | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42751958 | |||||||
| chr1:42752231 | C | T | 8 | a0001c0007t0001g0196 a0001c0007t0001g0203 a0001c0007t0001g0204 others(5): Show |
9 | HG01243.hp1 HG02559.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1569+43G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42752231 | |||||||
| chr1:42752271 | T | C | 3 | a0001c0027t0001g0179 a0007c0012t0001g0157 a0007c0012t0001g0162 |
3 | HG00639.hp1 HG02280.hp2 HG03225.hp1 |
splice_region_variant&intron_variant | LOW | c.1569+3A>G | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 10/14 | chr1 | 42752271 | |||||||
| chr1:42752905 | A | T | 1 | a0001c0001t0001g0108 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1346-241T>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 8/14 | chr1 | 42752905 | |||||||
| chr1:42752948 | C | T | 3 | a0001c0027t0001g0179 a0007c0012t0001g0157 a0007c0012t0001g0162 |
3 | HG00639.hp1 HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1346-284G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 8/14 | chr1 | 42752948 | |||||||
| chr1:42753224 | A | G | 1 | a0001c0001t0002g0195 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1346-560T>C | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 8/14 | chr1 | 42753224 | |||||||
| chr1:42753230 | A | G | 1 | a0003c0003t0003g0217 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1346-566T>C | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 8/14 | chr1 | 42753230 | |||||||
| chr1:42753321 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1346-657C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 8/14 | chr1 | 42753321 | |||||||
| chr1:42753693 | C | T | 3 | a0001c0008t0001g0045 a0001c0008t0001g0160 a0001c0008t0001g0161 |
4 | HG01243.hp1 HG02970.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1346-1029G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 8/14 | chr1 | 42753693 | |||||||
| chr1:42753724 | C | T | 1 | a0001c0001t0002g0155 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1346-1060G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 8/14 | chr1 | 42753724 | |||||||
| chr1:42753821 | G | A | 1 | a0001c0001t0001g0027 | 3 | HG01167.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1345+1048C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 8/14 | chr1 | 42753821 | |||||||
| chr1:42753831 | G | A | 10 | a0003c0003t0003g0028 a0003c0003t0003g0216 a0003c0003t0003g0217 others(7): Show |
12 | HG00738.hp2 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.1345+1038C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 8/14 | chr1 | 42753831 | |||||||
| chr1:42753895 | C | T | 2 | a0001c0001t0002g0165 a0015c0015t0002g0051 |
2 | NA18995.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1345+974G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 8/14 | chr1 | 42753895 | |||||||
| chr1:42753996 | C | T | 12 | a0001c0001t0001g0010 a0001c0001t0001g0038 a0001c0001t0001g0040 others(9): Show |
19 | HG00438.hp1 HG00673.hp2 HG02074.hp2 others(16): Show |
intron_variant | MODIFIER | c.1345+873G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 8/14 | chr1 | 42753996 | |||||||
| chr1:42753997 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1345+872C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 8/14 | chr1 | 42753997 | |||||||
| chr1:42754244 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1345+625C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 8/14 | chr1 | 42754244 | |||||||
| chr1:42754456 | G | T | 8 | a0002c0002t0001g0012 a0002c0002t0001g0016 a0002c0002t0001g0043 others(5): Show |
16 | HG00642.hp1 HG01074.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.1345+413C>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 8/14 | chr1 | 42754456 | |||||||
| chr1:42754605 | A | G | 2 | a0001c0014t0002g0214 a0001c0014t0002g0215 |
2 | NA18970.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1345+264T>C | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 8/14 | chr1 | 42754605 | |||||||
| chr1:42754644 | C | T | 1 | a0001c0023t0001g0150 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1345+225G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 8/14 | chr1 | 42754644 | |||||||
| chr1:42755320 | C | T | 1 | a0001c0001t0002g0170 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1171-103G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 6/14 | chr1 | 42755320 | |||||||
| chr1:42755447 | G | C | 5 | a0001c0001t0001g0020 a0001c0001t0001g0070 a0001c0001t0001g0107 others(2): Show |
7 | NA18942.hp1 NA18947.hp2 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.1170+101C>G | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 6/14 | chr1 | 42755447 | |||||||
| chr1:42755516 | C | T | 8 | a0002c0002t0001g0012 a0002c0002t0001g0016 a0002c0002t0001g0043 others(5): Show |
16 | HG00642.hp1 HG01074.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.1170+32G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 6/14 | chr1 | 42755516 | |||||||
| chr1:42755763 | GCT | G | 14 | a0001c0010t0002g0030 a0001c0010t0002g0059 a0003c0003t0003g0028 others(11): Show |
17 | HG00738.hp2 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.1081-128_1081-127d others(4): Show |
P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 5/14 | chr1 | 42755763 | |||||||
| chr1:42755815 | G | A | 1 | a0001c0001t0002g0185 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1081-178C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 5/14 | chr1 | 42755815 | |||||||
| chr1:42755966 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1081-329C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 5/14 | chr1 | 42755966 | |||||||
| chr1:42756076 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1081-439A>G | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 5/14 | chr1 | 42756076 | |||||||
| chr1:42756349 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1081-712C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 5/14 | chr1 | 42756349 | |||||||
| chr1:42756356 | C | T | 2 | a0001c0001t0002g0154 a0001c0001t0002g0169 |
2 | HG00544.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.1081-719G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 5/14 | chr1 | 42756356 | |||||||
| chr1:42756548 | T | A | 1 | a0001c0001t0002g0195 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1081-911A>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 5/14 | chr1 | 42756548 | |||||||
| chr1:42756597 | G | A | 3 | a0001c0010t0002g0030 a0001c0010t0002g0059 a0013c0024t0002g0058 |
4 | HG02970.hp1 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1081-960C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 5/14 | chr1 | 42756597 | |||||||
| chr1:42756768 | C | T | 9 | a0002c0002t0001g0012 a0002c0002t0001g0016 a0002c0002t0001g0043 others(6): Show |
17 | HG00642.hp1 HG01074.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.1080+1015G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 5/14 | chr1 | 42756768 | |||||||
| chr1:42757180 | TACAATGA others(9): Show |
T | 1 | a0001c0001t0001g0118 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1080+587_1080+602d others(18): Show |
P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 5/14 | chr1 | 42757180 | |||||||
| chr1:42757510 | A | G | 2 | a0001c0001t0001g0037 a0001c0001t0001g0083 |
3 | NA18963.hp1 NA18985.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1080+273T>C | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 5/14 | chr1 | 42757510 | |||||||
| chr1:42757636 | C | T | 10 | a0001c0023t0001g0150 a0002c0002t0001g0012 a0002c0002t0001g0016 others(7): Show |
18 | HG00642.hp1 HG01074.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.1080+147G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 5/14 | chr1 | 42757636 | |||||||
| chr1:42757668 | T | C | 1 | a0001c0001t0001g0027 | 3 | HG01167.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1080+115A>G | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 5/14 | chr1 | 42757668 | |||||||
| chr1:42757974 | T | G | 12 | a0001c0001t0001g0011 a0001c0001t0001g0036 a0001c0001t0001g0050 others(9): Show |
18 | HG00642.hp2 HG01884.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.941-52A>C | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 4/14 | chr1 | 42757974 | |||||||
| chr1:42758015 | C | G | 3 | a0001c0008t0001g0045 a0001c0008t0001g0160 a0001c0008t0001g0161 |
4 | HG01243.hp1 HG02970.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.941-93G>C | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 4/14 | chr1 | 42758015 | |||||||
| chr1:42758190 | G | A | 1 | a0001c0001t0002g0175 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.941-268C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 4/14 | chr1 | 42758190 | |||||||
| chr1:42758260 | T | C | 1 | a0001c0001t0002g0176 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.941-338A>G | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 4/14 | chr1 | 42758260 | |||||||
| chr1:42758319 | A | G | 164 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.941-397T>C | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 4/14 | chr1 | 42758319 | |||||||
| chr1:42758352 | A | C | 1 | a0001c0001t0001g0118 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.941-430T>G | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 4/14 | chr1 | 42758352 | |||||||
| chr1:42758762 | T | C | 1 | a0001c0001t0001g0201 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.940+90A>G | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 4/14 | chr1 | 42758762 | |||||||
| chr1:42759151 | T | C | 1 | a0002c0028t0001g0221 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.808+50A>G | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 3/14 | chr1 | 42759151 | |||||||
| chr1:42759437 | C | A | 3 | a0001c0010t0002g0030 a0001c0010t0002g0059 a0013c0024t0002g0058 |
4 | HG02970.hp1 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.619-47G>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 2/14 | chr1 | 42759437 | |||||||
| chr1:42759605 | T | C | 1 | a0001c0007t0001g0196 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.619-215A>G | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 2/14 | chr1 | 42759605 | |||||||
| chr1:42759981 | C | CT | 101 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(98): Show |
206 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.619-592dupA | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 2/14 | chr1 | 42759981 | |||||||
| chr1:42759981 | C | CTT | 13 | a0001c0001t0001g0069 a0001c0001t0001g0074 a0001c0001t0001g0092 others(10): Show |
13 | HG00280.hp2 HG00621.hp2 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.619-593_619-592dup others(2): Show |
P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 2/14 | chr1 | 42759981 | |||||||
| chr1:42759981 | CT | C | 16 | a0001c0001t0002g0047 a0001c0001t0002g0198 a0001c0007t0001g0203 others(13): Show |
25 | HG00323.hp1 HG00642.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.619-592delA | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 2/14 | chr1 | 42759981 | |||||||
| chr1:42760047 | C | A | 1 | a0001c0001t0002g0165 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.619-657G>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 2/14 | chr1 | 42760047 | |||||||
| chr1:42760235 | C | T | 3 | a0001c0001t0001g0036 a0001c0001t0001g0097 a0001c0001t0001g0098 |
4 | HG02080.hp2 HG02257.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.619-845G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 2/14 | chr1 | 42760235 | |||||||
| chr1:42760416 | A | G | 1 | a0001c0001t0002g0166 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.619-1026T>C | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 2/14 | chr1 | 42760416 | |||||||
| chr1:42760455 | T | C | 11 | a0003c0003t0003g0028 a0003c0003t0003g0216 a0003c0003t0003g0217 others(8): Show |
13 | HG00738.hp2 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.619-1065A>G | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 2/14 | chr1 | 42760455 | |||||||
| chr1:42760610 | A | T | 2 | a0001c0001t0001g0096 a0001c0001t0001g0119 |
2 | NA19072.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.619-1220T>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 2/14 | chr1 | 42760610 | |||||||
| chr1:42760665 | T | G | 128 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(125): Show |
246 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.619-1275A>C | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 2/14 | chr1 | 42760665 | |||||||
| chr1:42760806 | C | T | 1 | a0001c0001t0004g0029 | 3 | HG02896.hp1 HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.619-1416G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 2/14 | chr1 | 42760806 | |||||||
| chr1:42760896 | G | A | 3 | a0001c0001t0001g0066 a0001c0001t0001g0129 a0001c0001t0002g0146 |
3 | HG02071.hp1 HG02683.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.618+1427C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 2/14 | chr1 | 42760896 | |||||||
| chr1:42760903 | T | C | 3 | a0001c0008t0001g0045 a0001c0008t0001g0160 a0001c0008t0001g0161 |
4 | HG01243.hp1 HG02970.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.618+1420A>G | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 2/14 | chr1 | 42760903 | |||||||
| chr1:42760913 | A | G | 1 | a0002c0028t0001g0221 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.618+1410T>C | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 2/14 | chr1 | 42760913 | |||||||
| chr1:42760976 | C | CT | 123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(120): Show |
238 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.618+1346dupA | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 2/14 | chr1 | 42760976 | |||||||
| chr1:42760976 | C | CTT | 9 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0065 others(6): Show |
12 | HG01167.hp1 HG01928.hp2 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.618+1345_618+1346d others(4): Show |
P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 2/14 | chr1 | 42760976 | |||||||
| chr1:42760988 | T | C | 1 | a0001c0001t0002g0134 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.618+1335A>G | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 2/14 | chr1 | 42760988 | |||||||
| chr1:42761095 | G | A | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG00609.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.618+1228C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 2/14 | chr1 | 42761095 | |||||||
| chr1:42761098 | T | G | 1 | a0003c0003t0003g0217 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.618+1225A>C | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 2/14 | chr1 | 42761098 | |||||||
| chr1:42761117 | A | G | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(144): Show |
268 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.618+1206T>C | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 2/14 | chr1 | 42761117 | |||||||
| chr1:42761203 | T | C | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(144): Show |
268 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.618+1120A>G | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 2/14 | chr1 | 42761203 | |||||||
| chr1:42761226 | T | C | 1 | a0001c0014t0002g0215 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.618+1097A>G | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 2/14 | chr1 | 42761226 | |||||||
| chr1:42761269 | C | A | 1 | a0001c0023t0001g0150 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.618+1054G>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 2/14 | chr1 | 42761269 | |||||||
| chr1:42761285 | T | C | 2 | a0001c0001t0002g0048 a0001c0001t0002g0194 |
3 | HG02055.hp1 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.618+1038A>G | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 2/14 | chr1 | 42761285 | |||||||
| chr1:42761290 | T | C | 1 | a0001c0001t0001g0033 | 2 | HG01175.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.618+1033A>G | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 2/14 | chr1 | 42761290 | |||||||
| chr1:42761332 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.618+991T>C | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 2/14 | chr1 | 42761332 | |||||||
| chr1:42761413 | T | G | 1 | a0001c0001t0002g0177 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.618+910A>C | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 2/14 | chr1 | 42761413 | |||||||
| chr1:42761469 | A | T | 5 | a0001c0001t0001g0011 a0001c0001t0001g0055 a0001c0001t0001g0092 others(2): Show |
9 | HG00642.hp2 HG01884.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.618+854T>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 2/14 | chr1 | 42761469 | |||||||
| chr1:42761548 | A | G | 1 | a0013c0024t0002g0058 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.618+775T>C | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 2/14 | chr1 | 42761548 | |||||||
| chr1:42761747 | A | G | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(144): Show |
268 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.618+576T>C | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 2/14 | chr1 | 42761747 | |||||||
| chr1:42761855 | C | A | 1 | a0002c0002t0001g0149 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.618+468G>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 2/14 | chr1 | 42761855 | |||||||
| chr1:42761857 | G | A | 1 | a0001c0010t0002g0059 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.618+466C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 2/14 | chr1 | 42761857 | |||||||
| chr1:42762158 | C | T | 1 | a0001c0001t0001g0035 | 2 | HG01069.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.618+165G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 2/14 | chr1 | 42762158 | |||||||
| chr1:42762196 | G | A | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(144): Show |
268 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.618+127C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 2/14 | chr1 | 42762196 | |||||||
| chr1:42762709 | T | A | 1 | a0001c0001t0002g0184 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.466-234A>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42762709 | |||||||
| chr1:42762911 | G | T | 1 | a0001c0013t0001g0041 | 2 | HG03654.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.466-436C>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42762911 | |||||||
| chr1:42762999 | C | T | 1 | a0006c0006t0001g0034 | 2 | NA18948.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.466-524G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42762999 | |||||||
| chr1:42763000 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.466-525C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42763000 | |||||||
| chr1:42763014 | A | G | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(144): Show |
268 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.466-539T>C | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42763014 | |||||||
| chr1:42763045 | A | G | 3 | a0001c0001t0001g0063 a0001c0001t0001g0090 a0001c0001t0001g0091 |
3 | HG03490.hp2 HG03491.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.466-570T>C | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42763045 | |||||||
| chr1:42763091 | A | G | 3 | a0001c0008t0001g0045 a0001c0008t0001g0160 a0001c0008t0001g0161 |
4 | HG01243.hp1 HG02970.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.466-616T>C | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42763091 | |||||||
| chr1:42763195 | A | G | 1 | a0001c0001t0004g0029 | 3 | HG02896.hp1 HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.466-720T>C | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42763195 | |||||||
| chr1:42763237 | T | C | 5 | a0001c0001t0002g0013 a0001c0001t0002g0185 a0001c0001t0002g0202 others(2): Show |
9 | HG02145.hp1 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.466-762A>G | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42763237 | |||||||
| chr1:42763248 | G | C | 1 | a0005c0005t0003g0139 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.466-773C>G | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42763248 | |||||||
| chr1:42763388 | G | A | 9 | a0002c0002t0001g0012 a0002c0002t0001g0016 a0002c0002t0001g0043 others(6): Show |
17 | HG00642.hp1 HG01074.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.466-913C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42763388 | |||||||
| chr1:42763517 | C | A | 4 | a0001c0001t0001g0055 a0001c0001t0002g0008 a0001c0001t0002g0053 others(1): Show |
10 | HG02451.hp2 HG02717.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.466-1042G>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42763517 | |||||||
| chr1:42763548 | C | T | 35 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(32): Show |
69 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.466-1073G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42763548 | |||||||
| chr1:42763554 | C | A | 1 | a0001c0027t0001g0179 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.466-1079G>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42763554 | |||||||
| chr1:42763585 | T | G | 3 | a0001c0027t0001g0179 a0007c0012t0001g0157 a0007c0012t0001g0162 |
3 | HG00639.hp1 HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.466-1110A>C | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42763585 | |||||||
| chr1:42763604 | G | A | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG00609.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.466-1129C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42763604 | |||||||
| chr1:42763659 | G | A | 2 | a0001c0007t0001g0196 a0001c0007t0001g0203 |
2 | HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.466-1184C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42763659 | |||||||
| chr1:42763672 | C | CA | 26 | a0001c0001t0001g0027 a0001c0001t0001g0055 a0001c0001t0001g0197 others(23): Show |
41 | HG00597.hp2 HG00735.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.466-1198dupT | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42763672 | |||||||
| chr1:42763672 | CA | C | 72 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(69): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.466-1198delT | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42763672 | |||||||
| chr1:42763672 | CAA | C | 34 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0018 others(31): Show |
65 | HG00323.hp2 HG00423.hp1 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.466-1199_466-1198d others(4): Show |
P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42763672 | |||||||
| chr1:42763779 | T | C | 4 | a0001c0001t0002g0187 a0004c0004t0002g0026 a0004c0004t0002g0158 others(1): Show |
6 | HG00280.hp1 NA18939.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.466-1304A>G | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42763779 | |||||||
| chr1:42763861 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.466-1386C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42763861 | |||||||
| chr1:42763873 | G | A | 1 | a0005c0005t0003g0189 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.466-1398C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42763873 | |||||||
| chr1:42763897 | C | A | 1 | a0001c0001t0001g0127 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.466-1422G>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42763897 | |||||||
| chr1:42763930 | G | A | 6 | a0001c0001t0001g0190 a0001c0001t0002g0057 a0001c0001t0002g0211 others(3): Show |
6 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.466-1455C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42763930 | |||||||
| chr1:42764010 | A | G | 1 | a0001c0001t0001g0072 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.466-1535T>C | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42764010 | |||||||
| chr1:42764117 | C | T | 12 | a0001c0001t0001g0144 a0001c0001t0001g0197 a0001c0001t0001g0206 others(9): Show |
17 | HG01074.hp1 HG02015.hp2 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.466-1642G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42764117 | |||||||
| chr1:42764174 | C | T | 3 | a0001c0001t0002g0015 a0001c0001t0002g0151 a0001c0001t0002g0159 |
6 | HG00741.hp1 HG01099.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.466-1699G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42764174 | |||||||
| chr1:42764423 | C | CA | 11 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(8): Show |
12 | HG01928.hp1 HG02055.hp1 HG02735.hp2 others(9): Show |
intron_variant | MODIFIER | c.466-1949dupT | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42764423 | |||||||
| chr1:42764423 | CA | C | 19 | a0001c0001t0001g0018 a0001c0001t0001g0065 a0001c0001t0001g0066 others(16): Show |
22 | HG00639.hp1 HG01167.hp2 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.466-1949delT | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42764423 | |||||||
| chr1:42764441 | A | AG | 21 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0042 others(18): Show |
42 | HG00140.hp1 HG00140.hp2 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.466-1967_466-1966i others(3): Show |
P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42764441 | |||||||
| chr1:42764441 | A | G | 22 | a0001c0001t0001g0027 a0001c0001t0001g0050 a0001c0001t0001g0144 others(19): Show |
30 | HG01074.hp1 HG01167.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.466-1966T>C | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42764441 | |||||||
| chr1:42764465 | G | A | 1 | a0001c0001t0002g0195 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.466-1990C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42764465 | |||||||
| chr1:42764541 | A | T | 19 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0042 others(16): Show |
39 | HG00140.hp1 HG00140.hp2 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.465+1966T>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42764541 | |||||||
| chr1:42764766 | C | A | 5 | a0001c0007t0001g0196 a0001c0007t0001g0203 a0001c0007t0001g0204 others(2): Show |
5 | HG02559.hp2 HG02809.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+1741G>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42764766 | |||||||
| chr1:42764888 | C | T | 98 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(95): Show |
186 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.465+1619G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42764888 | |||||||
| chr1:42765060 | C | T | 1 | a0001c0001t0002g0135 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.465+1447G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42765060 | |||||||
| chr1:42765249 | G | A | 1 | a0003c0003t0003g0220 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.465+1258C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42765249 | |||||||
| chr1:42765256 | C | T | 2 | a0001c0001t0002g0134 a0001c0013t0001g0041 |
3 | HG03654.hp2 HG04228.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.465+1251G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42765256 | |||||||
| chr1:42765303 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.465+1204G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42765303 | |||||||
| chr1:42765501 | T | A | 1 | a0001c0001t0001g0197 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.465+1006A>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42765501 | |||||||
| chr1:42765614 | G | T | 1 | a0001c0001t0001g0062 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.465+893C>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42765614 | |||||||
| chr1:42765749 | C | G | 1 | a0001c0001t0001g0061 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.465+758G>C | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42765749 | |||||||
| chr1:42765804 | G | A | 1 | a0001c0001t0002g0198 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.465+703C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42765804 | |||||||
| chr1:42765861 | C | T | 2 | a0001c0001t0001g0022 a0001c0001t0001g0210 |
4 | HG02738.hp1 HG03688.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.465+646G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42765861 | |||||||
| chr1:42766015 | CCG | C | 105 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(102): Show |
205 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.465+490_465+491del others(2): Show |
P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42766015 | |||||||
| chr1:42766016 | CG | C | 8 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0027 others(5): Show |
15 | HG00741.hp2 HG01099.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.465+490delC | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42766016 | |||||||
| chr1:42766017 | G | A | 9 | a0001c0010t0002g0030 a0001c0010t0002g0059 a0003c0003t0003g0028 others(6): Show |
12 | HG01243.hp2 HG01981.hp1 HG02896.hp2 others(9): Show |
intron_variant | MODIFIER | c.465+490C>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42766017 | |||||||
| chr1:42766017 | G | C | 37 | a0001c0001t0001g0144 a0001c0001t0001g0190 a0001c0001t0001g0197 others(34): Show |
46 | HG00639.hp1 HG01074.hp1 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.465+490C>G | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42766017 | |||||||
| chr1:42766018 | C | G | 96 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(93): Show |
183 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.465+489G>C | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42766018 | |||||||
| chr1:42766019 | C | A | 1 | a0001c0001t0001g0210 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.465+488G>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42766019 | |||||||
| chr1:42766021 | C | A | 12 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0050 others(9): Show |
34 | HG00140.hp1 HG00140.hp2 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.465+486G>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42766021 | |||||||
| chr1:42766021 | C | CA | 4 | a0001c0001t0001g0206 a0001c0001t0002g0207 a0001c0001t0002g0208 others(1): Show |
4 | HG02145.hp1 HG02572.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.465+485_465+486ins others(1): Show |
P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42766021 | |||||||
| chr1:42766021 | CCA | C | 9 | a0001c0010t0002g0030 a0001c0010t0002g0059 a0003c0003t0003g0028 others(6): Show |
12 | HG01243.hp2 HG01981.hp1 HG02896.hp2 others(9): Show |
intron_variant | MODIFIER | c.465+484_465+485del others(2): Show |
P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42766021 | |||||||
| chr1:42766023 | A | C | 5 | a0001c0001t0002g0057 a0001c0001t0002g0211 a0001c0001t0002g0212 others(2): Show |
5 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+484T>G | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42766023 | |||||||
| chr1:42766025 | A | C | 4 | a0001c0001t0002g0057 a0001c0001t0002g0211 a0001c0001t0002g0212 others(1): Show |
4 | HG01884.hp2 HG02055.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.465+482T>G | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42766025 | |||||||
| chr1:42766026 | C | A | 3 | a0001c0001t0002g0211 a0001c0001t0002g0212 a0001c0001t0002g0213 |
3 | HG01884.hp2 HG02055.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.465+481G>T | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42766026 | |||||||
| chr1:42766127 | A | G | 1 | a0001c0001t0002g0056 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.465+380T>C | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42766127 | |||||||
| chr1:42766405 | C | T | 4 | a0001c0001t0001g0055 a0001c0001t0002g0008 a0001c0001t0002g0053 others(1): Show |
10 | HG02451.hp2 HG02717.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.465+102G>A | P3H1 | ENSG00000117385.16 | transcript | ENST00000296388.10 | protein_coding | 1/14 | chr1 | 42766405 |